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超乎肉眼所见。

Beyond what the eye can see.

作者信息

Ahmad Kate E, Fraser Clare L, Sue Carolyn M, Barton Jason J S

机构信息

Department of Neurology, Royal North Shore Hospital, Sydney, Australia.

Save Sight Institute, University of Sydney, Sydney, Australia.

出版信息

Surv Ophthalmol. 2016 Sep-Oct;61(5):674-9. doi: 10.1016/j.survophthal.2016.02.003. Epub 2016 Feb 26.

Abstract

A 45-year-old woman presented with acute sequential optic neuropathy resulting in bilateral complete blindness. No significant visual recovery occurred. Past medical history was relevant for severe preeclampsia with resultant renal failure, diabetes mellitus, and sudden bilateral hearing loss when she was 38 years old. There was a family history of diabetes mellitus in her mother. Testing for common causes of bilateral optic neuropathy did not reveal a diagnosis for her illness. The maternal and personal history of diabetes and deafness prompted testing for mitochondrial disease. The 3 primary mitochondrial DNA mutations responsible for Leber hereditary optic neuropathy were absent, but the patient was subsequently found to have a disease causing mitochondrial DNA mutation, m.13513G>A. The case illustrates the importance of early testing for mitochondrial disease and demonstrates that Leber hereditary optic neuropathy-like presentations may be missed if testing is limited to the 3 primary mutations.

摘要

一名45岁女性出现急性连续性视神经病变,导致双眼完全失明,视力未出现明显恢复。既往病史显示,她曾患严重先兆子痫并导致肾衰竭、糖尿病,38岁时突然出现双侧听力丧失。她的母亲有糖尿病家族史。对双侧视神经病变的常见病因进行检测后,未明确其病情诊断。其母亲和本人患糖尿病及耳聋的病史促使对线粒体疾病进行检测。虽然未检测到导致Leber遗传性视神经病变的3种主要线粒体DNA突变,但该患者随后被发现患有由线粒体DNA突变m.13513G>A引起的疾病。该病例说明了早期检测线粒体疾病的重要性,并表明如果检测仅限于3种主要突变,可能会漏诊Leber遗传性视神经病变样表现。

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